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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948457Generated: November 1, 2026

N-Iodosuccinimide → Ethyl 4-iodo-5-phenylisoxazole-3-carboxylate

https://huagongshe.com/reaction/1948457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantEthyl 5-phenylisoxazole-3-carboxylateHCID 571142—
SolventTrifluoroacetic acidHCID 6422—
ProductEthyl 4-iodo-5-phenylisoxazole-3-carboxylateHCID 58537206152.2%

Reaction Steps

Large Scale: A mixture of ethyl 5-phenylisoxazole-3-carboxylate (3.05 g, 14.0 mmol) and N-iodosuccinimide (3.79 g, 16 9 mmol) in trifluoroacetic acid (78 mL) was stirred at room temperature for 3.5 h. The volatiles were removed under reduced pressure, and the residue was partitioned between ethyl acetate (150 mL) and water (150 mL). The organic layer was washed with a 1N aqueous solution of sodium hydroxide (150 mL), washed with a 3% aqueous solution of sodium bisulfate (2×150 mL), washed with brine (150 mL), and dried over anhydrous magnesium sulfate. Concentration under reduced pressure afforded ethyl 4-iodo-5-phenylisoxazole-3-carboxylate (4.69 g, 13.7 mmol, 97% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399451B2
Source datasetuspto-grants-2013_03
ORD IDord-435c688f03644f3c828025655b39809e
Source noteuspto-grants-2013_03